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    Treprostinil Sodium

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    UNITED THERAPEUTICS CORPORATION

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    UNITED THERAPEUTICS CORPORATION

    U.S.A
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    Pharmtech & Ingredients
    Not Confirmed
    • fda
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    Regulatory Info : Prescription

    Registration Country : Canada

    TREPROSTINIL (TREPROSTINIL SODIUM)

    Brand Name : REMODULIN

    Dosage Form : SOLUTION

    Dosage Strength : 1MG/ML

    Packaging : 20ML

    Approval Date :

    Application Number : 2246552

    Regulatory Info : Prescription

    Registration Country : Canada

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    02

    UNITED THERAPEUTICS CORPORATION

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    UNITED THERAPEUTICS CORPORATION

    U.S.A
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    Pharmtech & Ingredients
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    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : Prescription

    Registration Country : Canada

    TREPROSTINIL (TREPROSTINIL SODIUM)

    Brand Name : REMODULIN

    Dosage Form : SOLUTION

    Dosage Strength : 2.5MG/ML

    Packaging : 20ML

    Approval Date :

    Application Number : 2246553

    Regulatory Info : Prescription

    Registration Country : Canada

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    03

    UNITED THERAPEUTICS CORPORATION

    U.S.A
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    UNITED THERAPEUTICS CORPORATION

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    Regulatory Info : Prescription

    Registration Country : Canada

    TREPROSTINIL (TREPROSTINIL SODIUM)

    Brand Name : REMODULIN

    Dosage Form : SOLUTION

    Dosage Strength : 5MG/ML

    Packaging : 20ML

    Approval Date :

    Application Number : 2246554

    Regulatory Info : Prescription

    Registration Country : Canada

    blank

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    Product Web Link

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    04

    UNITED THERAPEUTICS CORPORATION

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    UNITED THERAPEUTICS CORPORATION

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : Prescription

    Registration Country : Canada

    TREPROSTINIL (TREPROSTINIL SODIUM)

    Brand Name : REMODULIN

    Dosage Form : SOLUTION

    Dosage Strength : 10MG/ML

    Packaging : 20ML

    Approval Date :

    Application Number : 2246555

    Regulatory Info : Prescription

    Registration Country : Canada

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